• Director of Clinical Research Consulting

    Vitalief (New Brunswick, NJ)
    …working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong ... business and domain expertise to provide more efficient, higher-quality clinical trials and unmatched value to Sponsors,...and fluent in all activities required for preparing a clinical trial for Site Activation: IRB Submission… more
    Vitalief (07/31/25)
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  • Clinical Lead, Early Clinical

    Sanofi Group (Morristown, NJ)
    …development, which require a scientifically inquisitive, energetic and proactive person. + Ensure Clinical Trial standards are maintained at the site and in ... Operations and Evidence Generation & Decision Science), Early Development Clinical Operations (EDCO, including Clinical Trial...Experience in the design and execution of early development clinical trials (phase 1a/b and 2a) and… more
    Sanofi Group (07/29/25)
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  • Future Talent Program - Clinical Sciences…

    Merck (Rahway, NJ)
    Clinical Sciences and Study Management is a group within the Global Clinical Trials Operations department which focuses on the planning, execution and close ... out of clinical trials within a program. ...out of clinical trials within a program. Clinical ...with the planning, execution and/or close out of a clinical trial (s). The candidate will be an… more
    Merck (08/21/25)
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  • Senior Director, Global Clinical

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    clinical stages to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is ... refine a clinical development strategy. + Designing clinical trials for the purpose of meeting...integrity of the methodology and ensure the safety of clinical subjects. + Leading clinical trial more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Manager Clinical Study Lead (oncology)

    Regeneron Pharmaceuticals (Warren, NJ)
    …oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. ... Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + Ensures… more
    Regeneron Pharmaceuticals (08/02/25)
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  • Sr. Medical Director, Clinical Development…

    Bristol Myers Squibb (Princeton, NJ)
    …regulatory authority interactions, design and execution of Phase 1 to Phase 3 clinical trials , and medical monitoring. This role works collaboratively with ... clinical study reports, and review of other clinical trial and regulatory documents + Conduct...Data Review and Independent Data Monitoring Committees + Conduct clinical trials using ethical guidelines relevant to… more
    Bristol Myers Squibb (07/08/25)
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  • Senior Manager Clinical Study Lead…

    Regeneron Pharmaceuticals (Warren, NJ)
    …and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. ... Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + Ensures… more
    Regeneron Pharmaceuticals (07/30/25)
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  • Global Clinical Supply Regions Head…

    Merck (Rahway, NJ)
    Clinical Trial Operations (GCTO) team in conducting our company's clinical trials . **Major Activities and Responsibilities:** + Active member of GCS ... and countries to support the execution of our company's Clinical trials (300+studies) portfolio globally across more..._Supply_ as well as support & training to Global Clinical Trial Operations + Lead the development… more
    Merck (08/26/25)
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  • Senior Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong ... documents, study documents and forms. + Schedules and conducts trial visits by informing patients and coordinating procedures per...to thrive in a fast-paced environment working on multiple clinical trials concurrently. + Must have strong… more
    Vitalief (07/12/25)
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  • Clinical Research Coordinator

    Actalent (New Brunswick, NJ)
    Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various ... + Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and...patients with study sponsors and input data into the clinical trials database. + Maintain comprehensive research… more
    Actalent (09/04/25)
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